Clinical challenges in interpreting multiple pathogenic mutations in single patients

BACKGROUND: In the past two decades, genetic testing for cancer risk assessment has entered mainstream clinical practice due to the availability of low-cost panels of multiple cancer-associated genes. However, the clinical value of multiple-gene panels for cancer susceptibility is not well establish...

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Detalles Bibliográficos
Autores principales: Slaught, Christa, Berry, Elizabeth G., Bacik, Lindsay, Skalet, Alison H., Anadiotis, George, Tuohy, Therese, Leachman, Sancy A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863461/
https://www.ncbi.nlm.nih.gov/pubmed/33541411
http://dx.doi.org/10.1186/s13053-021-00172-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863461/
https://www.ncbi.nlm.nih.gov/pubmed/33541411
http://dx.doi.org/10.1186/s13053-021-00172-3

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